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Triethylamine → 5-Bromo-2-chloro-N-(5-methoxy-1H-pyrazol-3-yl)pyrimidin-4-amine

HRID 415438
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인쇄 미리보기

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HRID 415438 반응식
[Br:1][C:2]1[C:3](Cl)=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.[CH3:10][O:11][C:12]1[NH:16][N:15]=[C:14]([NH2:17])[CH:13]=1.C(N(CC)CC)C>C1COCC1>[Br:1][C:2]1[C:3]([NH:17][C:14]2[CH:13]=[C:12]([O:11][CH3:10])[NH:16][N:15]=2)=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 2899735-Bromo-2,4-dichloropyrimidineHCID 178493288HCID 178493288, 화합물

생성물 1

HCID 1784930715-Bromo-2-chloro-N-(5-methoxy-1H-pyrazol-3-yl)pyrimidin-4-amine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
40 °C

실험 절차

To a solution of 5-bromo-2,4-dichloropyrimidine (1.20 g, 5.26 mmol) in THF (10 ml) at room temperature was added 5-methoxy-1H-pyrazol-3-amine (594 mg, 5.26 mmol) and triethylamine (685 mg, 6.3 mmol) and the reaction mixture was stirred at 40° C. overnight. The suspension was filtered and washed with water and dried to give the desired product as a white solid. MS: 305 (M+1).

후처리

  1. filtrationThe suspension was filtered
  2. washwashed with water
  3. customdried

출처 및 근거

ORD 기록
ord-5adb43e3db0440bc98e8ae9ccbf71f87
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08088784B2

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